Grace M Tannin

Associate Professor (Nontenured Clinical), Pediatrics
Endocrinology

Emailgrace.tannin@utsouthwestern.edu

Source: Scopus
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717 Citations
9 h-Index
12 Article
2 Letter

Topical triamcinolone induced Cushing syndrome: A case report
Taylor, O., Mejia-Otero, J. D., Tannin, G. M. & Gordon, K., May 1 2020, In: Pediatric dermatology. 37, 3, p. 582-584 3 p.
Research output: Contribution to journal › Article › peer-review
A novel syndrome of generalized lipodystrophy associated with pilocytic astrocytoma
Patni, N., Alves, C., Von Schnurbein, J., Wabitsch, M., Tannin, G. M., Rakheja, D. & Garg, A., Oct 1 2015, In: Journal of Clinical Endocrinology and Metabolism. 100, 10, p. 3603-3606 4 p.
Research output: Contribution to journal › Article › peer-review
10 Scopus citations
Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure
Harrison, S. M., Campbell, I. M., Keays, M., Granberg, C. F., Villanueva, C., Tannin, G., Zinn, A. R., Castrillon, D. H., Shaw, C. A., Stankiewicz, P. & Baker, L. A., Oct 1 2013, In: American Journal of Medical Genetics, Part A. 161, 10, p. 2487-2494 8 p.
Research output: Contribution to journal › Article › peer-review
19 Scopus citations
Lower Extremity Venous Obstruction Secondary to Congenital Bladder Diverticulum
Miller, M., Baker, L. A., Tannin, G. & Koral, K., May 1 2007, In: Journal of Urology. 177, 5, 1 p.
Research output: Contribution to journal › Article › peer-review

1 Scopus citations
Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene
Kayes-Wandover, K. M., Tannin, G. M., Shulman, D., Peled, D., Jones, K. L., Karaviti, L. & White, P. C., 2001, In: Journal of Clinical Endocrinology and Metabolism. 86, 11, p. 5379-5382 4 p.
Research output: Contribution to journal › Article › peer-review

Open Access
17 Scopus citations

Topical triamcinolone induced Cushing syndrome: A case report

A novel syndrome of generalized lipodystrophy associated with pilocytic astrocytoma

Screening and familial characterization of copy-number variations in NR5A1 in 46,XY disorders of sex development and premature ovarian failure

Lower Extremity Venous Obstruction Secondary to Congenital Bladder Diverticulum

Congenital hyperreninemic hypoaldosteronism unlinked to the aldosterone synthase (CYP11B2) gene